Avoid costly REC and recruitment delays and by ensuring your trial documents resonate with the patients they're meant to serve.
Are you struggling with participant recruitment, retention, or ethics committee approval for your clinical trials?
Most Participant Information Sheets and Informed Consent Forms (PIS/ICFs) are written by academic and medical experts who use complex language and terminology that participants find difficult to understand.
Ethics committees now actively recommend PIS/ICF reviews by the general public and potential trial patients.
Our PPIE consultants provide expert patient-centered document reviews based on unrivalled experience with diverse patient groups across numerous therapeutic areas.
We offer a completely free introductory consultation meeting to address your individual needs. Sign up by filling in the quick form here:
1. Document submission — We securely store your trial ICFs in our protected database
2. Reviewer selection — We contact reviewers from our database with relevant condition experience
3. Confidentiality assurance — All reviewers sign NDAs to maintain strict confidentiality standards
4. Structured feedback — Our reviewers access documents via secure channels and provide detailed insights
5. Expert compilation — Our PPIE Coordinator collates all reviewer feedback into actionable recommendations
6. Timely delivery — Comprehensive report returned within 10-15 days, ready for implementation
Want to know more about our patient review service?
Download our comprehensive service brochure for detailed information on our methodology, case studies, and pricing:
Our extensive network of patient reviewers spans numerous therapeutic areas, providing authentic perspectives from people with lived experience:
Everyone should have equal opportunity to understand and participate in clinical research, regardless of their background or condition.